Petros Syrris

16.5k total citations
126 papers, 7.8k citations indexed

About

Petros Syrris is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Orthopedics and Sports Medicine. According to data from OpenAlex, Petros Syrris has authored 126 papers receiving a total of 7.8k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Cardiology and Cardiovascular Medicine, 48 papers in Molecular Biology and 22 papers in Orthopedics and Sports Medicine. Recurrent topics in Petros Syrris's work include Cardiomyopathy and Myosin Studies (67 papers), Cardiovascular Effects of Exercise (57 papers) and Sports injuries and prevention (22 papers). Petros Syrris is often cited by papers focused on Cardiomyopathy and Myosin Studies (67 papers), Cardiovascular Effects of Exercise (57 papers) and Sports injuries and prevention (22 papers). Petros Syrris collaborates with scholars based in United Kingdom, Italy and United States. Petros Syrris's co-authors include William J. McKenna, Srijita Sen‐Chowdhry, Perry Elliott, Deirdre Ward, Angeliki Asimaki, Nicholas D. Carter, Siân Hughes, Antonios Pantazis, Alison Evans and Sharon Jenkins and has published in prestigious journals such as The Lancet, Circulation and Nature Communications.

In The Last Decade

Petros Syrris

123 papers receiving 7.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Petros Syrris United Kingdom 48 5.9k 1.9k 1.5k 459 454 126 7.8k
Leon A. Bach Australia 43 811 0.1× 2.6k 1.4× 462 0.3× 834 1.8× 313 0.7× 154 6.3k
W. Charles O’Neill United States 48 528 0.1× 1.7k 0.9× 267 0.2× 826 1.8× 175 0.4× 115 5.8k
Keiko Uchida Japan 35 484 0.1× 1.8k 0.9× 114 0.1× 565 1.2× 251 0.6× 233 4.9k
Domenico Corradi Italy 34 2.3k 0.4× 747 0.4× 172 0.1× 1.8k 4.0× 573 1.3× 128 5.5k
Ken Tsuchiya Japan 32 450 0.1× 964 0.5× 109 0.1× 697 1.5× 283 0.6× 241 4.2k
N. Cary United Kingdom 23 734 0.1× 612 0.3× 84 0.1× 1.6k 3.4× 409 0.9× 53 3.2k
Francesco Tona Italy 29 1.9k 0.3× 373 0.2× 53 0.0× 958 2.1× 484 1.1× 147 3.4k
Pablo García‐Pavía Spain 39 2.4k 0.4× 3.0k 1.6× 128 0.1× 577 1.3× 624 1.4× 244 5.5k
Marie‐Christine Vantyghem France 35 452 0.1× 1.2k 0.7× 48 0.0× 2.0k 4.3× 393 0.9× 224 4.6k
Dominique Prié France 38 125 0.0× 905 0.5× 225 0.1× 858 1.9× 249 0.5× 121 4.2k

Countries citing papers authored by Petros Syrris

Since Specialization
Citations

This map shows the geographic impact of Petros Syrris's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Petros Syrris with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Petros Syrris more than expected).

Fields of papers citing papers by Petros Syrris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Petros Syrris. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Petros Syrris. The network helps show where Petros Syrris may publish in the future.

Co-authorship network of co-authors of Petros Syrris

This figure shows the co-authorship network connecting the top 25 collaborators of Petros Syrris. A scholar is included among the top collaborators of Petros Syrris based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Petros Syrris. Petros Syrris is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Monda, Emanuele, Athanasios Bakalakos, Douglas Cannie, et al.. (2024). Prevalence of Pathogenic Variants in Cardiomyopathy-Associated Genes in Acute Myocarditis. JACC Heart Failure. 12(6). 1101–1111. 22 indexed citations
2.
Cannie, Douglas, Kush Patel, Alexandros Protonotarios, et al.. (2024). Prevalence of transthyretin cardiac amyloidosis in patients with high-degree AV block. Open Heart. 11(1). e002606–e002606. 3 indexed citations
3.
Monda, Emanuele, Athanasios Bakalakos, Douglas Cannie, et al.. (2024). Prevalence of pathogenic variants in cardiomyopathy-associated genes in acute myocarditis: a systematic review and meta-analysis. European Heart Journal. 45(Supplement_1). 1 indexed citations
4.
Monda, Emanuele, Athanasios Bakalakos, Robin Lachmann, et al.. (2024). Incidence and risk factors for development of left ventricular hypertrophy in Fabry disease. Heart. 110(12). 846–853. 6 indexed citations
5.
Monda, Emanuele, Athanasios Bakalakos, Petros Syrris, et al.. (2023). Cardiovascular involvement in later-onset malonyl-CoA decarboxylase deficiency: Case studies and literature review. European Journal of Medical Genetics. 66(12). 104885–104885. 1 indexed citations
6.
James, Cynthia A., Jan D.H. Jongbloed, Ray E. Hershberger, et al.. (2021). International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework. Circulation Genomic and Precision Medicine. 14(3). e003273–e003273. 110 indexed citations
7.
Hughes, Rebecca, Claudia Camaioni, João B. Augusto, et al.. (2021). Myocardial Perfusion Defects in Hypertrophic Cardiomyopathy Mutation Carriers. Journal of the American Heart Association. 10(15). e020227–e020227. 31 indexed citations
8.
Hall, Charlotte, Henry Sutanto, Chrysoula Dalageorgou, et al.. (2018). Frequency of genetic variants associated with arrhythmogenic right ventricular cardiomyopathy in the genome aggregation database. European Journal of Human Genetics. 26(9). 1312–1318. 26 indexed citations
9.
Lopes, Luís R., Petros Syrris, Chrysoula Dalageorgou, et al.. (2015). Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy. European Journal of Medical Genetics. 58(11). 611–616. 25 indexed citations
10.
Behr, Elijah R., Paula L. Hedley, Petros Syrris, et al.. (2010). Abstract 16108: Mutations in the Lamin A/C Gene Play a Major Role in Sudden Arrhythmic Death Syndrome. Circulation. 122(5). 716–24. 1 indexed citations
11.
Gehmlich, Katja, Petros Syrris, Emma Peskett, et al.. (2010). Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations. Cardiovascular Research. 90(1). 77–87. 41 indexed citations
12.
Behr, Elijah R., Paula L. Hedley, Petros Syrris, et al.. (2010). Mutations in the Lamin A/C Gene Play a Major Role in Sudden Arrhythmic Death Syndrome. UCL Discovery (University College London). 1 indexed citations
13.
Syrris, Petros, et al.. (2008). Novel TFAP2B Mutation in Nonsyndromic Patent Ductus Arteriosus. Genetic Testing. 12(3). 457–459. 21 indexed citations
14.
Limongelli, Giuseppe, et al.. (2006). Mutation screening of the PTPN11 gene in hypertrophic cardiomyopathy. European Journal of Medical Genetics. 49(5). 426–430. 10 indexed citations
15.
Sen‐Chowdhry, Srijita, Petros Syrris, William J. McKenna, et al.. (2006). Letter regarding article by Norman et al, "Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy" - Response. UCL Discovery (University College London).
16.
Sen‐Chowdhry, Srijita, Sanjay Prasad, Petros Syrris, et al.. (2006). Cardiovascular Magnetic Resonance in Arrhythmogenic Right Ventricular Cardiomyopathy Revisited. Journal of the American College of Cardiology. 48(10). 2132–2140. 145 indexed citations
17.
Heathcote, Kirsten, Claire Braybrook, Michelle Guy, et al.. (2005). Common arterial trunk associated with a homeodomain mutation of NKX2.6. Human Molecular Genetics. 14(5). 585–593. 49 indexed citations
18.
Ladusans, E J, et al.. (2003). Predictive testing for the long QT syndrome in children and teenagers - Whose best interests are served?. UCL Discovery (University College London).
19.
Syrris, Petros, Nicholas D. Carter, & Michael A. Patton. (1999). Novel nonsense mutation of the endothelin-B receptor gene in a family with Waardenburg-Hirschsprung disease. American Journal of Medical Genetics. 87(1). 69–71. 55 indexed citations
20.
Hagger, R, et al.. (1998). Are there c-kit gene mutations in chronic idiopathic constipation?. Gastroenterology. 114. A797–A797. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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